Description of the disease * EnglishPolish Pobierz sekcję do PDF Definition A rare multiple congenital anomalies/dysmorphic syndrome characterized by microcephaly, developmental delay and intellectual disability, postnatal growth retardation, dysmorphic craniofacial features (including sloping forehead, beaked nose, large and protruding ears, micrognathia, high-arched palate, and craniosynostosis), immunologic abnormalities with transient hypogammaglobulinemia in infancy and defective chemotaxis leading to recurrent infections, as well as autoimmune/autoinflammatory phenomena. Skeletal anomalies and hypogonadism have also been reported. Disease data Classification Malformation syndrome Synonyms Microcephaly-hypogammaglobulinemia-abnormal immunity syndrome Małogłowie - hipogammaglobulinemia - nieprawidłowa odporność ORPHA code 3132 OMIM code 251240 ICD10 code Q87.8 ICD11 code 4A01.0Y *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl